98509-03-6Relevant articles and documents
Julia olefination as a general route to phenyl (α-fluoro)vinyl sulfones
He, Maggie,Ghosh, Arun K.,Zajc, Barbara
experimental part, p. 999 - 1004 (2009/04/04)
Mild and efficient synthesis of phenyl (α-fluoro)vinyl sulfones via condensation of aldehydes and a ketone with a novel benzothiazolyl based bis-sulfone reagent is reported and this proceeds with moderate to good Z-stereoselectivity. Georg Thieme Verlag Stuttgart.
A Novel and Efficient Synthesis of Fluoromethyl Phenyl Sulphone and Its Use as a Fluoromethyl Wittig Equivalent
Inbasekaran, Muthiah,Peet, Norton P.,McCarthy James R.,LeTourneau, Michael E.
, p. 678 - 679 (2007/10/02)
A new synthesis of fluoromethyl phenyl sulphone (2) and the reaction of its conjugate base (3) with carbonyl compounds provides β-fluoro-alcohols (5), which are utilized to prepare terminal vinyl fluorides (8) via α-fluoro-α,β-unsaturated sulphones (6).